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Two newly established cell lines derived from the same colonic adenocarcinoma exhibit differences in EGF-receptor ligand and adhesion molecule expression

Two newly established cell lines derived from the same colonic adenocarcinoma exhibit differences in EGF-receptor ligand and adhesion molecule expression
Two newly established cell lines derived from the same colonic adenocarcinoma exhibit differences in EGF-receptor ligand and adhesion molecule expression
Two morphologically distinct cell lines, GP2d and GP5d, derived from the same adenocarcinoma of the colon, have been established and characterised. Both clones have the same genetic changes, consistent with the usual pattern of tumour progression in colon cancer. The cells also have an inverted duplication of bands 10q11 to 10q21, but Southern blot analysis failed to identify any translocations involving the ret protooncogene, which maps to this region. GP2d grew by spreading from the edges of microcolonies to form a confluent layer of cells. GP5d grew in discrete islands of cells forming multilayered colonies. These differing patterns of growth correlated with variation in expression or cellular distribution of ?2-integrin, desmoplakin and e-cadherin. Only GP2d responded to exogenously added epidermal growth factor (EGF), transforming growth factor-alpha (TGF?) or insulin with an increase in cell numbers, even though both cell lines possessed similar numbers of EGF receptors. Analysis of EGF receptor ligand expression showed that GP5d cells expressed relatively more TGF? mRNA than did GP2d; in contrast, amphiregulin mRNA, which was abundant in GP2d, was virtually undetectable in GP5d. Even though GP5d failed to exhibit a growth response to EGF, it underwent a marked epithelial-mesenchymal transition when treated with EGF, indicating separation of growth and morphological responses to EGF.
0020-7136
48-57
Solic, Nicola
e8808086-3cda-43c1-a122-681908c9a4f3
Collins, Jane E.
be0e66f1-3036-47fa-9d7e-914c48710ba4
Richter, Audrey
5b4fb888-b3a7-4b81-a8a7-ffd2c046a196
Holt, Susan J.
e7082707-6349-4a6e-854f-a529c3904c2b
Campbell, Ian
4933e498-792b-4064-9ac8-edfa56713765
Alexander, Peter
9b0e0950-b6fa-414e-8bc0-c259dea3f36d
Davies, Donna E.
7de8fdc7-3640-4e3a-aa91-d0e03f990c38
Solic, Nicola
e8808086-3cda-43c1-a122-681908c9a4f3
Collins, Jane E.
be0e66f1-3036-47fa-9d7e-914c48710ba4
Richter, Audrey
5b4fb888-b3a7-4b81-a8a7-ffd2c046a196
Holt, Susan J.
e7082707-6349-4a6e-854f-a529c3904c2b
Campbell, Ian
4933e498-792b-4064-9ac8-edfa56713765
Alexander, Peter
9b0e0950-b6fa-414e-8bc0-c259dea3f36d
Davies, Donna E.
7de8fdc7-3640-4e3a-aa91-d0e03f990c38

Solic, Nicola, Collins, Jane E., Richter, Audrey, Holt, Susan J., Campbell, Ian, Alexander, Peter and Davies, Donna E. (1995) Two newly established cell lines derived from the same colonic adenocarcinoma exhibit differences in EGF-receptor ligand and adhesion molecule expression. International Journal of Cancer, 62 (1), 48-57. (doi:10.1002/(ISSN)1097-0215). (PMID:7601566)

Record type: Article

Abstract

Two morphologically distinct cell lines, GP2d and GP5d, derived from the same adenocarcinoma of the colon, have been established and characterised. Both clones have the same genetic changes, consistent with the usual pattern of tumour progression in colon cancer. The cells also have an inverted duplication of bands 10q11 to 10q21, but Southern blot analysis failed to identify any translocations involving the ret protooncogene, which maps to this region. GP2d grew by spreading from the edges of microcolonies to form a confluent layer of cells. GP5d grew in discrete islands of cells forming multilayered colonies. These differing patterns of growth correlated with variation in expression or cellular distribution of ?2-integrin, desmoplakin and e-cadherin. Only GP2d responded to exogenously added epidermal growth factor (EGF), transforming growth factor-alpha (TGF?) or insulin with an increase in cell numbers, even though both cell lines possessed similar numbers of EGF receptors. Analysis of EGF receptor ligand expression showed that GP5d cells expressed relatively more TGF? mRNA than did GP2d; in contrast, amphiregulin mRNA, which was abundant in GP2d, was virtually undetectable in GP5d. Even though GP5d failed to exhibit a growth response to EGF, it underwent a marked epithelial-mesenchymal transition when treated with EGF, indicating separation of growth and morphological responses to EGF.

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Published date: 4 July 1995

Identifiers

Local EPrints ID: 179813
URI: http://eprints.soton.ac.uk/id/eprint/179813
ISSN: 0020-7136
PURE UUID: 16fc8db4-8d69-4e4b-8186-380821367090
ORCID for Donna E. Davies: ORCID iD orcid.org/0000-0002-5117-2991

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Date deposited: 06 Apr 2011 10:50
Last modified: 15 Mar 2024 02:35

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Contributors

Author: Nicola Solic
Author: Jane E. Collins
Author: Audrey Richter
Author: Susan J. Holt
Author: Ian Campbell
Author: Peter Alexander
Author: Donna E. Davies ORCID iD

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